| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21752 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:46364080-46366820 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr22:46366752-46366763 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr22:46366752-46366762 | GCCCCGCCCC | + | 6.02 | | RREB1 | MA0073.1 | chr22:46366414-46366434 | CCCCAACCCCCCCACTTCCC | + | 6.08 | | RREB1 | MA0073.1 | chr22:46366406-46366426 | ACCCCAACCCCCAACCCCCC | + | 6.41 | | SP3 | MA0746.2 | chr22:46366751-46366764 | TGCCCCGCCCCCC | + | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I045966 | chr22 | 46362089 | 46369100 |
|
Enhancer Sequence | TGAGAGTCAT CTCCTCTGGG AAGCCCTCTG AGATGCCCTA GGGGGTCCAC CACTCCTTCC 60
TGAATGAACA CAGCCACTGG GCCTCCCTCT GTGCTGCCTG TGGCCAACCT CCCTGTTCCT 120
GATAGCTGAG AATGGCCTGT CTCCTGCACA CCGACCACAC CAGGCATCAA GCTAGAGCTT 180
CCCACAGCCA CCCGGTGAGG TTTGTGCTCC CGTGATCTGC ACTGGAGAGG GAAGAGCTGG 240
GCCTTGGGAC ACAGCCAGGC AGTGAGGGCC CTGTGGAGTC AGGATGAGGA CCCAGATCTG 300
AGTCACTATC ATGCCCTTTG GCCTCACGGG AAACCATGTT AGAAAACGGC GCATTATCCT 360
ACAGGCCTCA GTGCACAACC GTGGAGTCCA GCGTCACCCC AGGACCTCCT GTCCTCCCTC 420
TGCACACAGA CGGTCCAGGA TGCACATTCT CCCCTTTAGC CAATGGTTGT TGGGTCTCGT 480
CCACCTGGTG ATGAGTTCTG GGGAGTTTCC TGTGATTAGG GAGGCTCCAC TTGCCCACCT 540
CCAGTGGGGG GTCCCCAGTT GAGATCTCAT CAGATTTCCC AGCTTGAACC CCACATGCAC 600
ACCCTCTATG GAACGTTCTA CACTTTCAAG TGCCAACTAC ACGTGGCCTG ATCTGAGCCT 660
TGGGAGAGGG ATCACCATCC CAAGTGACCC ATGAGGAGAC TGAGGCCCAG AGAGGCTCAT 720
GGACCTGCTC AGGGCACACA GCAGAGCCCC TCCCAGACCT GGATAGACGC AGACCCTCCA 780
GGCTGGGAGT TGCCCCTCCC CCAAGGGCAA CCTGAACACG CCTGAGCCAC GGGGCGCATC 840
CTGTCCCCAC ACGGGCCATG GTGCCATGGG AGTAGGCCTG GTTCATCTCC TCCCCCTCGA 900
GGGTCATGGC CACAGCACTT CTGGGACTGT GGCTGGCACC GCTGACAAAG CCACAGCGGT 960
GGAGCCGGGA AGAGGCCTGG CCTGGCGGGG CCGTGGTAAG TGCCCCCCCA CCCTGCCACA 1020
GCCAGGTGGT CGGTGAGTAA CCGCCCCGTC ACCCATGACT CACTTGGCTC CCCAGAGCAG 1080
GCGGTCACCA TGACAGGCTC CTACCGGAAG ACCTGGGGGG GTCGTCAGAG CCAACCCCCA 1140
CATCTGGGAG AGGAAGACTG AGAGCGGAAG AGACCTGCCT GGGACAGAAG CGCAGCCTGG 1200
TCCTGGTCAA GGCCTCAGCC AGGCCCCCAT TGCAGCTGAC CCAGCACCAC AAGCCTTCCT 1260
CTTGGCCTGC AGTCCCCTAC CTGCCCTCCC TTGGGCCCTT ACTGACCCCC GCTGGCCCTG 1320
GGAGCTCCTG CACTGACAAC AGAGCTCTGC ACAGAGAAGG CGAGGGCTGG CCAGAGCCGC 1380
CTAGCACGGC TGCAAGTCAG CATGTAGCAG GGGCGCAGGG CGCTTCCAGG CCAACACACC 1440
CGTCCAACCT GATCAGTGGC AGGGGCCCAG GCATGCGTCT GGGATTCGGT GTGCACCGAC 1500
CACAGCCCAG GACAGGGAGC TAGAGGAGCA GTCCAGATGA AAGGGGGAGG ATCAGCTGTC 1560
AGCCAGCGTC TGGGATCCCA GCAATGGGAT CTGGAAAGCT CCTGAAAGTT CTCTGGAGCA 1620
GAATGAAGCC TCCACCCAGC GACCCTCCTA GCCCAGGCAT CCTCAGATCC AAAGGCCAAT 1680
GCCATCGAGT GCGCCTGCAG TGCTGAGGGT CGGCTGACAC TCACCCCCAC CTCTCACAGC 1740
TCTCCAAGCA CTTGCTGCTG GCTGCCTCCC CCAAGTGCAG CCATCGGGTC AGAGACATCG 1800
AAACCAAGGT CTTCTCACTT TGCATGCTTT CATTCAAACC GAATCGCGCA GGCCCTACTC 1860
CCATCTATGG TCAGCCTTGC GCCCACCAAA CAAACCGGGC AAGGGAAATC TGAGACCCAC 1920
CCCCCTCACT CCGGGAACGT GTCTGGGTTC CTCTCCGCTT GGGGAAGGCT GGCGTCAGCG 1980
TCTTCCTCCC TGTGGGGCAG GAGCTACTGA GGGCAAGTCA GGGATGCAGT CTGCCTTCCT 2040
GTCCCCGACG ACCCAGGCCA GACCCCAGCA CTGGCCCAGG GATGCCTGGA AAAACTGTTT 2100
CCTTAGGAGA ATTTCTGCCA ACACAGCTGG GCAGTGCACA CTCCAGGAGC AAGCCTGGCG 2160
GGGGTAGTCA CTGCAGGCCC GGATGAGGGG CCAGCCCTGA GGTAAACCCG GGGTCTGCAG 2220
AGGTACACTG GGCACCACCT TGCCCCAGAG GCCCCTCACT GCTGCCTTGG CATCAACTCC 2280
CACCAGGCTT CTGGGGCCCC TGCGCACCTC CCTCTCTCCG ACCCTTACCC CAACCCCCAA 2340
CCCCCCCACT TCCCTTGCCT CCACCTCCGC AGGACTCCTG GTCTCCCACC CCGGACACCT 2400
CTCTATGAAC ACCGAACCTC AGCCAGCCGG CTCCAAAACT GATTTCCCAA GCACCGGAGC 2460
TGCCAATTCT CTAGCAAGGC CTAAGGCTGA AACGCCAGGA TTCTGGGGAG GGGGAGGCTT 2520
CCTGGCCTCC AACCGCTAGA CGCTGAAATT CCAAAGTCCC CTGGTTGATC CAGTTCCTGG 2580
AAAGGACACC AGAAGCAGGA CCCAGGGACC CTGGCACTTT ATCAGCCTGG GTCCCCACTG 2640
CTCAGGCGGT CCCCACCCGC ATGCGCCCTG CTGCCCCGCC CCCCTCAGGC GATGCCTCCG 2700
CAGCCGGGGC TGCCCGCCGG GCCTGGAGCG CTCTCTGTGC 2740
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